BHI AGAR
K-Number: K834319 · 1984-01-13
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Device Summary
Frequently Asked Questions
What is the BHI AGAR?
BHI AGAR is a medical device that received FDA 510(k) clearance on 1984-01-13. The listed applicant is Hardy Media. The 510(k) number is K834319.
When did BHI AGAR receive FDA 510(k) clearance?
BHI AGAR received FDA 510(k) clearance on 1984-01-13, under 510(k) number K834319.
Who is the listed applicant for BHI AGAR?
The FDA 510(k) record lists Hardy Media as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BHI AGAR?
The FDA product code for BHI AGAR is JSG.
Other records listing Hardy Media as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: JSG)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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